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1 ycins, in particular in the formation of the alicyclic 6-hydroxy function of the landomycin aglycon.
2 hat enzymes are used for fatty, aromatic and alicyclic acid degradation versus for benzoate and cyclo
3 alogues, consisting of aliphatic carbamates, alicyclic amides, and heteroaromatic amides, were synthe
4  metal-free methods are accommodated and the alicyclic amine nucleophiles used here are unprecedented
5 e also described, including benzyl azide and alicyclic amine nucleophiles.
6 version of C-H bonds to C-C bonds on various alicyclic amine scaffolds.
7 te ions, primary aliphatic amines, secondary alicyclic amines (5H(+) only), and OH(-) (5H(+) only) we
8                               Functionalized alicyclic amines are important building blocks for the s
9 h to selectively manipulate the C-H bonds of alicyclic amines at sites remote to nitrogen.
10          The synthesis of valuable bioactive alicyclic amines containing variable substituents in mul
11                                          The alicyclic amines displayed structural preference.
12  primary aliphatic and a series of secondary alicyclic amines in 50% MeCN-50% water (v/v) at 25 degre
13 )Z)CH(3)) by primary aliphatic and secondary alicyclic amines in 50% MeCN-50% water (v/v) at 25 degre
14 log k0 for the reaction of 4H with secondary alicyclic amines in water (1.22) is 1.81 log units highe
15 idene Meldrum's acids (2-SMe-Z) by secondary alicyclic amines occurs by a three-step mechanism.
16 ha-C-H bond functionalization of unprotected alicyclic amines remain rare.
17  a-C-H bond functionalization of unprotected alicyclic amines remain rare.
18 ular functionalization of the y-C-H bonds in alicyclic amines to install C(sp(3) )-halogen, oxygen, n
19  new strategy to access alpha-functionalized alicyclic amines via their corresponding imine-BF(3) com
20 -(2-bis(4-fluorophenyl)methyl)sulfinyl)alkyl alicyclic amines were synthesized and evaluated for bind
21  Saturated nitrogen-containing heterocycles (alicyclic amines) feature prominently in pharmaceuticals
22 y OH(-), primary aliphatic amines, secondary alicyclic amines, and carboxylate ions have been determi
23  (4H) by primary aliphatic amines, secondary alicyclic amines, hydroxide ion, and water in water at 2
24  the C-H bond functionalization of feedstock alicyclic amines, the simultaneous introduction of more
25 xylate ions, primary aliphatic and secondary alicyclic amines, water and OH(-) in 50% MeCN-50% water
26  of bis(4-fluorophenyl)methyl)sulfinyl)alkyl alicyclic amines, where the piperazine-2-propanol scaffo
27 ew advance in this area utilizes N-lithiated alicyclic amines.
28 drogenative coupling approach to incorporate alicyclic amino residues into the structure of model cyc
29                                   However, N-alicyclic aminomethylene bisphosphonates, such as incadr
30  chemical structures of a range of synthetic alicyclic and aromatic acids and their acute toxicities
31 d straight-chained, branched, double-bonded, alicyclic, and aromatic features.
32 hly unsaturated polyphenols, carboxylic-rich alicyclic, and nitrogen-containing formulae.
33 ation/functionalization of various aliphatic/alicyclic/aromatic carboxamide systems.
34                      Analogues incorporating alicyclic beta-amino acids exhibited diverse receptor bi
35                     Computational studies of alicyclic carbodiimides (RN horizontal lineC horizontal
36  the only biomolecule class with contiguous, alicyclic carbon backbones of this size.
37 -H arylation/acetoxylation of aliphatic- and alicyclic carboxamides afforded the corresponding beta-C
38 -directed arylation/benzylation of aliphatic/alicyclic carboxamides and benzamides were ascertained f
39 lyst, aryl component of AC, nucleophile, and alicyclic component of AC on the desired FC reactivity.
40 rivatives, together with high percentages of alicyclic compounds (triterpenoids, steroids, or tocophe
41 allenging C(sp(3))-rich molecules, including alicyclic compounds bearing multiple contiguous stereoce
42 ne)Ru(II) precursors; thus, the isolation of alicyclic cyclohexadienone derivatives upon demetalation
43 the two different classes of epoxides, i.e., alicyclic (cyclohexene oxide) and aliphatic (propylene o
44                A common reaction pathway for alicyclic (cyclohexene oxide) and aliphatic (propylene o
45              The conformationally restricted alicyclic derivatives were not only more cytotoxic than
46     We have found that several aliphatic and alicyclic diols induce melanogenesis in cultured S91 mou
47 f observed reduced compounds corresponded to alicyclic hydrocarbons in the size range C10 to C17.
48 roborate several recent studies that suggest alicyclic hydrocarbons to be important components of lon
49 in situ transformation of the latter into an alicyclic imine which undergoes selective C-C bond forma
50 find an explanation of the low reactivity of alicyclic ketones such as cyclohexanone in reactions wit
51 hat the widely discussed all carbon-backbone alicyclic model of CRAM is incompatible with the MS2 fra
52 ed a series of analogues of carboxylate-rich alicyclic molecules (CRAM), a molecular class hypothesiz
53 nin-derived compounds and/or carboxylic rich alicyclic molecules (CRAM).
54 he production of refractory, carboxylic-rich alicyclic molecules (CRAM).
55 e identified as carbohydrates, carboxyl-rich alicyclic molecules, and aliphatic molecules.
56 s dissolved black carbon and carboxylic-rich alicyclic molecules, was also rapidly and extensively re
57 frost thaw DOM directly showed carboxyl-rich alicyclic molecules, while the same components from lowe
58 ignin-like, tannin-like, and carboxylic-rich alicyclic molecules.
59 rther elaborations, providing functionalized alicyclic motifs and pharmacophores.
60 L(-1) of an OSPW subfraction containing only alicyclic NA, and considered by most authors to be NA se
61 ynthesis and characterization of a series of alicyclic organochalcogen compounds derived from 2-chlor
62         NMR investigations revealed that the alicyclic portion of the compounds thus formed displayed
63 e the cyclization reactions of the universal alicyclic precursor farnesyl pyrophosphate to produce mo
64  the exclusive formation of the dearomatized alicyclic products without subsequent rearomatization.
65 nted on alkynes bearing long alkyl chain, an alicyclic ring, hydroxy, ether, and ester functionality,
66 These observations are extended to C(3)-C(6) alicyclic rings containing these motifs and predict part
67 lkyl glycerol tetraethers (GDGTs with 0 to 8 alicyclic rings), including the complete resolution of G
68 .0.1(3,10).1(5,8)]dodecanes (DTDs) with rare alicyclic scaffolding in high overall yields.
69 of residue 92 leads to the production of the alicyclic sesquiterpenes (E)-beta- and (E,E)-alpha-farne
70 en replaced with Ala, produced almost 80% of alicyclic sesquiterpenes, suggesting an energetic separa
71 5-dimethoxybenzoic acid by making use of the alicyclic side chain in N as a "conformational lock".
72 l precursors, bridging arene feedstocks with alicyclic structures.
73                    Acyclic sulfones 4a-f and alicyclic sulfone 7 react with readily available N-acylb
74  VLCFA derivatives and less (if at all) with alicyclic wax constituents.